Entrez 6712 | Ensembl ENSG00000173898 | |
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Aliases SPTBN2, GTRAP41, SCA5, SCAR14, spectrin beta, non-erythrocytic 2 External IDs MGI: 1313261 HomoloGene: 48482 GeneCards: SPTBN2 |
Clinical significance
Mutations in this gene is associated with Spinocerebellar ataxia type 5.
Interactions
SPTBN2 has been shown to interact with:
References
SPTBN2 Wikipedia(Text) CC BY-SA